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62347-97-1

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62347-97-1 Usage

General Description

"[4-(Methylamino)-3-nitrophenyl]methanol is a compound with the chemical formula C9H10N2O3. It is a derivative of phenol, consisting of a phenyl ring with a nitro group at the 3-position and a methylamino group at the 4-position. This chemical is used in the synthesis of organic compounds and pharmaceuticals, and it has potential applications in the manufacturing of dyes and pigments. It is important to handle this compound with caution and in accordance with safety protocols, as it may pose health hazards if not used properly."

Check Digit Verification of cas no

The CAS Registry Mumber 62347-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,4 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62347-97:
(7*6)+(6*2)+(5*3)+(4*4)+(3*7)+(2*9)+(1*7)=131
131 % 10 = 1
So 62347-97-1 is a valid CAS Registry Number.

62347-97-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(Methylamino)-3-nitrophenyl]methanol

1.2 Other means of identification

Product number -
Other names 4-methylamino-3-nitrobenzyl alcohol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62347-97-1 SDS

62347-97-1Relevant articles and documents

BENZIMIDAZOLE DERIVATIVES AS BROMODOMAIN INHIBITORS

-

Page/Page column 70, (2016/10/24)

Compounds of formula (I) and salts thereof: wherein R1, R2, R3, R4 are defined herein. Compounds of formula (I) and salts thereof have been found to inhibit the binding of the BET family of bromodomain proteins to, for example, acetylated lysine residues and thus may have use in therapy, for example in the treatment of autoimmune and inflammatory diseases, such as rheumatoid arthritis; and cancers.

Artificial Redox Enzymes. 1. Synthetic Strategies

Rong, Ding,Ye, Hongping,Boehlow, Todd R.,D'Souza, Valerian T.

, p. 163 - 167 (2007/10/02)

Organic models of flavoenzymes consist of a binding site covalently attached to a flavin derivative acting as the catalytic site.The earlier reported synthesis of such a model using α-cyclodextrin as the binding site proved to be difficult to reproduce wi

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